24562-76-3 Usage
Uses
Used in Pharmaceutical Industry:
ETHYL 1,2,3,4-TETRAHYDROQUINOLINE-4-CARBOXYLATE is used as a building block for the synthesis of various pharmaceutical compounds due to its unique structure and functionality. It contributes to the development of new drugs by providing a foundation for chemical modifications and enhancements.
Used in Organic Synthesis:
In the field of organic synthesis, ETHYL 1,2,3,4-TETRAHYDROQUINOLINE-4-CARBOXYLATE serves as a precursor for the preparation of other organic molecules. Its versatile chemical nature allows for further reactions and transformations, leading to the creation of a wide range of organic compounds with diverse applications.
Used in Agrochemical Industry:
ETHYL 1,2,3,4-TETRAHYDROQUINOLINE-4-CARBOXYLATE may have potential utility in the agrochemical industry, where it could be employed as a component in the development of new agrochemical products. Its unique properties may contribute to the creation of more effective and environmentally friendly solutions for agricultural applications.
Used in Other Industries:
Beyond the pharmaceutical, organic synthesis, and agrochemical industries, ETHYL 1,2,3,4-TETRAHYDROQUINOLINE-4-CARBOXYLATE may also find applications in other fields. Its unique structure and functionality could be harnessed to develop new materials and products, further expanding its utility and impact across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 24562-76-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,6 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24562-76:
(7*2)+(6*4)+(5*5)+(4*6)+(3*2)+(2*7)+(1*6)=113
113 % 10 = 3
So 24562-76-3 is a valid CAS Registry Number.
24562-76-3Relevant academic research and scientific papers
Reduction of Quinolinecarboxylic Acids by Raney Alloy
Gracheva, I. N.,Tochilkin, A. I.
, p. 65 - 67 (2007/10/02)
The heterocyclic nucleus in quinolinecarboxylic acids is reduced by Raney alloy (nickel-aluminium) in alkaline media to give 1,2,3,4-tetrahydro-2-,3-,4-,5-,6-, and 8-quinolinecarboxylic acids and 8-methyl-5-quinolinecarboxylic acid and their ethyl esters.
